Affinity analysis of non-steady-state data obtained under mass transport limited conditions using BIAcore technology
- 1 September 1999
- journal article
- research article
- Published by Wiley in Journal of Molecular Recognition
- Vol. 12 (5) , 285-292
Abstract
Binding data obtained with Biacore instrumentation is often evaluated using a kinetic transport model where reaction rate constants and a mass transport coefficient are used to describe the interaction. Here the use of a simplified model, an affinity transport model, for determination of the affinity (KD) but not the kinetics (ka, kd) has been investigated. When binding rates were highly governed by mass transport effects the two models returned the same affinity and gave similar residuals, but ka and kd values found with the kinetic transport model were unreliable. On the other hand the affinity transport model failed to describe the data when binding curves were less influenced by mass transport effects. Under such circumstances the kinetic transport model returned correct ka and kd values. Depending on the outcome of the analysis the affinity transport model can therefore be used to reduce uncertainties of the kinetic parameters or as an easy way to determine KD values from non-steady-state data. The use of the affinity transport model is illustrated with simulated data and with binding data obtained for the interaction between a 439 Da thrombin inhibitor and immobilized thrombin. Since it is more difficult to resolve high ka values for low molecular weight analytes, the affinity transport model may be particularly useful for affinity analysis involving fast reactions between such analytes and immobilized protein targets. Copyright © 1999 John Wiley & Sons, Ltd.Keywords
This publication has 14 references indexed in Scilit:
- Nonspecific Amine Immobilization of Ligand Can Be a Potential Source of Error in BIAcore Binding Experiments and May Reduce Binding AffinitiesAnalytical Biochemistry, 1997
- Influence of mass transfer and surface ligand heterogeneity on quantitative BIAcoreTM binding data. Analysis of the interaction of NC10 Fab with an anti-idiotype Fab′Journal of Molecular Recognition, 1997
- Kinetic analysis of macromolecular interactions using surface plasmon resonance biosensorsCurrent Opinion in Biotechnology, 1997
- Experimental design for kinetic analysis of protein-protein interactions with surface plasmon resonance biosensorsJournal of Immunological Methods, 1997
- Surface Plasmon Resonance Detection and Multispot Sensing for Direct Monitoring of Interactions Involving Low-Molecular-Weight Analytes and for Determination of Low AffinitiesAnalytical Biochemistry, 1995
- Interpreting Complex Binding Kinetics from Optical Biosensors: A Comparison of Analysis by Linearization, the Integrated Rate Equation, and Numerical IntegrationAnalytical Biochemistry, 1995
- Kinetic and Concentration Analysis Using BIA TechnologyMethods, 1994
- Real‐time DNA binding measurements of the ETSl recombinant oncoproteins reveal significant kinetic differences between the p42 and p51 isoformsProtein Science, 1994
- Antigen-Antibody Binding and Mass Transport by Convection and Diffusion to a Surface: A Two-Dimensional Computer Model of Binding and Dissociation KineticsAnalytical Biochemistry, 1993
- Kinetic analysis of monoclonal antibody-antigen interactions with a new biosensor based analytical systemJournal of Immunological Methods, 1991